Evidence Level
Limited
1 Clinical Trial
4 Documented Benefits
2/5 Evidence Score

DL-185® is dileucine, a dipeptide of two L-leucine molecules (L-leucyl-L-leucine monohydrate). It was developed by Ingenious Ingredients LP, sold as RAMPS until 2024, and is now distributed by NNB Nutrition under the DL-185 name. Dipeptides are absorbed intact through the PEPT1 transporter in the gut, and a crossover trial in 10 young men confirmed intact dileucine reaches the bloodstream after a 2 g dose. A 10-week trial in 34 resistance-trained men then found 2 g/day increased leg press one-rep max compared with placebo and leg press reps to failure compared with leucine, with no group difference in bench press, body composition, jump height, anaerobic capacity or maximal voluntary contraction. That trial did not measure muscle protein synthesis. Both trials were funded by the company that developed the ingredient and neither has been repeated by an independent group. The figures of 185% faster absorption and 86% more leucine delivered come from supplier marketing material rather than from the published trial results, which reported the same plasma leucine exposure after dileucine and after leucine (p=0.396). Faster absorption is a pharmacokinetic measurement, not a benefit in itself.

Studied Dose 2 g/day for 10 weeks in the resistance-training strength trial; a single 2 g dose in the acute muscle protein synthesis trial.
Active Compound L-leucyl-L-leucine monohydrate, the dipeptide of two L-leucine molecules. Developed by Ingenious Ingredients LP, marketed as RAMPS until 2024, and now distributed by NNB Nutrition as DL-185®. Ingenious Ingredients holds a granted US patent (US11026991B2, granted 8 June 2021) whose first claim covers dileucine-plus-leucine compositions for increasing muscle protein synthesis, and its principals list further patent applications for dileucine in the disclosures of the trials they funded.

Benefits

Higher muscle protein synthesis than leucine in one 10-man trial

In a crossover trial, 10 healthy young men took 2 g of dileucine or 2 g of leucine on separate occasions. Cumulative myofibrillar protein synthesis over 3 hours rose with dileucine (0.075 %/h) but not with leucine (0.047 %/h, p=0.023), a difference of about 60% between the two means. Two limits matter. Plasma leucine exposure was the same after both drinks (p=0.396), so the extra synthesis was not explained by more leucine reaching the blood. And a protein synthesis rate measured in a muscle biopsy is a laboratory endpoint, not a gain in muscle size or strength. Ten participants, and the trial was funded by the company that developed the ingredient.

One leg press measure improved over 10 weeks

Thirty-four resistance-trained men, roughly 11 per group, trained 4 days a week for 10 weeks while taking 2 g/day of dileucine, 2 g/day of leucine or placebo. Leg press one-rep max increased more with dileucine than with placebo (p=0.02), and leg press reps to failure increased more with dileucine than with leucine (p=0.04). Nothing else separated the groups: bench press strength and endurance, body composition, anaerobic capacity, countermovement jump and maximal voluntary contraction all showed no group difference. The confidence interval on the leg press strength result was wide, from 5.8 to 73.2 kg, the groups were small, and the study was sponsored by the company that supplies the ingredient.

Muscle breakdown was measured and was not reduced

Two human dileucine trials measured muscle protein breakdown directly and neither found a reduction. In the 10-man crossover trial, mixed muscle protein breakdown was 0.043 %/h after leucine and 0.051 %/h after dileucine, with no difference between them (p=0.659). In the post-exercise trial, urinary 3-methylhistidine, a marker of myofibrillar breakdown, did not differ between a dileucine-containing amino acid drink, a BCAA drink and collagen (p=0.58). No trial has tested dileucine during dieting or caloric restriction, so there is no human evidence that it preserves muscle in a cut.

Not tested in older adults

Every published dileucine trial recruited young adults: 10 men averaging 23 years, 34 resistance-trained men averaging 28 years, and 12 recreationally active adults averaging 24 years. No trial has enrolled older adults, and none has measured muscle mass, strength or physical function in an older population. The absorption argument is a mechanism, not a result, and it has not been tested in aging muscle.

Mechanism of action

1

PEPT1 dipeptide transporter absorption

Free leucine crosses the intestinal brush border on amino acid carriers, chiefly B0AT1, while dipeptides use PEPT1, a separate proton-coupled peptide transporter. Dileucine does reach the blood intact: plasma dileucine rose further after dileucine than after leucine (p=0.013) in the 10-man crossover trial. What that trial did not show is more leucine in the blood, because plasma leucine exposure was the same after both drinks (p=0.396). PEPT1 is itself saturable, so this route has a ceiling too.

2

mTORC1 signalling: no measured difference from leucine

The 10-man crossover trial took muscle biopsies and measured mTORC1 signalling directly. Akt, rpS6 and p70S6K phosphorylation rose over time after leucine and after dileucine alike, with no separation between conditions, and 4E-BP1 phosphorylation did not change after either (p=0.229). The cell-culture arm of the 2025 trial also found no effect on p-RPS6 (p=0.39) or p-4E-BP1 (p=0.50). So the higher synthesis rate seen with dileucine was not matched by a stronger measured mTORC1 signal, and the mechanism is not yet explained.

Clinical trials

1
Dileucine vs Leucine vs Placebo for Strength After 10 Weeks of Resistance Training (RCT, sponsor-funded)
PubMed

Hagele AM et al., PLoS One 2024 (NCT06121869, registered retrospectively). Randomized, double-blind, placebo-controlled trial in 34 resistance-trained men taking 2 g/day dileucine monohydrate, 2 g/day leucine or placebo alongside a 4-day-per-week training programme for 10 weeks. Outcomes measured: leg press and bench press one-rep max and reps to failure, body composition, anaerobic capacity, countermovement jump, maximal voluntary contraction. Muscle protein synthesis was not measured. The material tested was branded RAMPS at the time and is the same dileucine now sold as DL-185; the sponsor was its developer, Ingenious Ingredients LP.

34 resistance-trained men, average age 28, about 11 per group. No women, no untrained people, no older adults.

Leg press one-rep max rose more with dileucine than with placebo (p=0.02; 95% CI 5.8 to 73.2 kg) and leg press reps to failure rose more with dileucine than with leucine (p=0.04). Every other comparison was null: bench press one-rep max and reps to failure, body composition, anaerobic capacity, countermovement jump and maximal voluntary contraction showed no group differences. Leucine beat neither placebo nor dileucine on any measure. One small sponsor-funded trial with about 11 men per group, with no independent replication.

Side effects and drug interactions

Common Potential side effects

No adverse effects were reported at 2 g/day, but the three published trials together enrolled 56 people for at most 10 weeks, which is far too little exposure to rule out uncommon or delayed effects
Leucine-leucine sequences occur in dietary protein and appear briefly during digestion, but taking an isolated 2 g dose of the free dipeptide every day is not the same exposure, and it has not been studied beyond 10 weeks
Only 56 people have taken dileucine in a published trial, all healthy adults in their twenties and only 4 of them women; it has not been studied in adolescents, in pregnancy or breastfeeding, or in people with kidney or liver disease

Important Drug interactions

No drug interaction study has been carried out with dileucine, so none is established either way; that is an absence of testing, not a finding of safety
Leucine and dileucine activate the mTOR pathway, so anyone taking an mTOR inhibitor such as sirolimus or everolimus, including transplant recipients, should ask their doctor first. This is a theoretical concern based on the pathway; no interaction has been tested in people.

Frequently asked questions about DL-185® (Dileucine)

What is DL-185?

DL-185® is dileucine, a dipeptide of two L-leucine molecules (L-leucyl-L-leucine monohydrate). It was developed by Ingenious Ingredients LP, sold as RAMPS until 2024, and is now distributed by NNB Nutrition under the DL-185 name.

What is DL-185 used for?

DL-185 is researched primarily for Athletic Performance and Muscle & Recovery. In a crossover trial, 10 healthy young men took 2 g of dileucine or 2 g of leucine on separate occasions. Cumulative myofibrillar protein synthesis over 3 hours rose with dileucine (0.075 %/h) but not with leucine (0.047 %/h, p=0.

What is the recommended dosage of DL-185?

The clinically studied dose is 2 g/day for 10 weeks in the resistance-training strength trial; a single 2 g dose in the acute muscle protein synthesis trial. Always follow the product label and check with a healthcare provider for personal advice.

Is DL-185 safe, and does it have side effects?

For most healthy adults, DL-185 is well tolerated at studied doses. Reported effects can include: No adverse effects were reported at 2 g/day, but the three published trials together enrolled 56 people for at most 10 weeks, which is far too little exposure to rule out uncommon or delayed effects Leucine-leucine sequences occur in dietary protein and appear briefly during dige… It may also interact with some medications. DL-185 is not right for everyone, so check with a healthcare provider first if you are pregnant or breastfeeding, have a medical condition, or take prescription medication.

Does DL-185 interact with any medications?

Possible interactions include: No drug interaction study has been carried out with dileucine, so none is established either way; that is an absence of testing, not a finding of safety Leucine and dileucine activate the mTOR pathway, so anyone taking an mTOR inhibitor such as sirolimus or everolimus, including… If you take prescription medication, check with a pharmacist or doctor before using it.

How strong is the scientific evidence for DL-185?

NutraSmarts rates the evidence for DL-185 as Limited (2 out of 5). It is backed by 1 clinical trial and 3 cited references summarized on this page. A higher rating reflects more, larger, and better-designed human studies.

References(3 citations)

Evidence ratings on NutraSmarts are based on the totality of human clinical research, with emphasis on randomized controlled trials, meta-analyses, and systematic reviews. The references below directly support claims made throughout this page.

  1. Paulussen KJM, Alamilla RA, Salvador AF, McKenna CF, Askow AT, Fang HY, et al. Dileucine ingestion is more effective than leucine in stimulating muscle protein turnover in young males: a double blind randomized controlled trial. J Appl Physiol (1985). 2021;131(3):1111-1122. doi: 10.1152/japplphysiol.00295.2021.PubMedUsed to support: Crossover trial in 10 healthy young men: a single 2 g dose of dileucine raised cumulative myofibrillar protein synthesis over 3 hours (0.075 %/h) while an equal 2 g dose of leucine did not (0.047 %/h, p=0.023). Plasma leucine exposure was the same after both drinks (p=0.396), muscle protein breakdown did not differ (p=0.659), and mTORC1 signalling rose similarly under both conditions with no change in 4E-BP1. Ten participants, a biopsy-measured synthesis rate rather than a strength or size outcome, and funded by the ingredient's developer.
  2. Hagele AM, Krieger JM, Gaige CJ, Holley KF, Gross KN, Iannotti JM, et al. Dileucine ingestion, but not leucine, increases lower body strength and performance following resistance training: A double-blind, randomized, placebo-controlled trial. PLoS One. 2024;19(12):e0312997. doi: 10.1371/journal.pone.0312997.PubMedUsed to support: 10-week trial in 34 resistance-trained men: 2 g/day dileucine increased leg press one-rep max versus placebo (p=0.02, 95% CI 5.8 to 73.2 kg) and leg press reps to failure versus leucine (p=0.04), while 2 g/day leucine beat nothing. Bench press strength and endurance, body composition, anaerobic capacity, countermovement jump and maximal voluntary contraction all showed no group difference, and muscle protein synthesis was not measured. About 11 men per group, registered retrospectively, and sponsored by Ingenious Ingredients LP, which developed the dileucine tested and whose principals are co-authors and hold the dileucine patent applications.
  3. Aguilera JA, Tinline-Goodfellow CT, Lees MJ, Kortebi I, West DWD, Abou Sawan S, et al. Dileucine-supplemented essential amino acids support whole-body anabolism after resistance exercise and serum-stimulated cell-based anabolism. J Int Soc Sports Nutr. 2025;22(1):2590090. doi: 10.1080/15502783.2025.2590090.PubMedUsed to support: Crossover trial in 12 young adults (8 men, 4 women) after a bout of resistance exercise, comparing three drinks developed by Iovate Health Sciences: an essential amino acid formula containing 2 g dileucine plus 1 g leucine and 9.15 g total EAA, a BCAA drink, and collagen. Exogenous leucine retention was the same for the dileucine formula and the BCAA drink (215.7 vs 219.2 micromol/kg, p=0.68), with both far above collagen. Urinary 3-methylhistidine, a muscle breakdown marker, did not differ between drinks (p=0.58). In an exploratory cell-culture arm the dileucine formula had no effect on puromycin incorporation (p=0.31), protein ubiquitination (p=0.59), mTORC1 substrate phosphorylation (p=0.39 and p=0.50) or myotube diameter (p=0.55), while a separate isotope-based synthesis measure only trended (p=0.086). Whole-body leucine retention is a surrogate, not a measured muscle outcome, and the product tested was a multi-ingredient blend from a different company, not the dileucine sold on its own.